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Growth of the maternal intestine during pregnancy and lactation [scRNA gut]

GSE247927 Mus musculus (mouse) Single-cell RNA-seq 17 samples Submitted 2025/03/20 Platform GPL17021Platform GPL30172
At a glance

Single-cell RNA-seq · mouse · 17 samples

What it is
Single-cell RNA-seqGene activity measured in thousands of individual cells, so cell types can be told apart.
Organism
Mus musculus (mouse)
Samples
17 samples: 11 × Lactating_WT vs 3 × Lactating_KO vs 3 × Virgin_WTGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Growth of the maternal intestine during reproductionCell · 2025
Summary (written by the submitters)
The organs of female animals can be dramatically enlarged and metabolically remodelled by reproduction. The cellular changes and genetic programmes that initiate and sustain these transformations remain largely uncharacterised. It is also unclear whether the mechanisms that drive reproductive growth are shared between organs, or with other environmental triggers of adult organ growth.
Read the full summary ↓
We have tackled these questions in mouse mothers, whose intestines provide a striking and genetically tractable example of reproductive organ resizing. We find that intestinal remodelling during reproduction is anticipatory of reproductive needs and distinct from diet-induced intestinal resizing.
Published in
Growth of the maternal intestine during reproduction
Ameku T, Laddach A, Beckwith H et al. · Cell 2025 · PMID 40112802 · doi:10.1016/j.cell.2025.02.015
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE247927_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: Single-cell studies usually ship their counts as 10x files (matrix.mtx, barcodes.tsv, features.tsv), an .h5 file, or an .rds / .h5ad object that Seurat or Scanpy can open. Look for those among the supplementary files.

Also filed as BioProject PRJNA1040924 and SRA study SRP472261. Searching any of these in the dataset finder brings you back here.

Study design
11 × Lactating_WT vs 3 × Lactating_KO vs 3 × Virgin_WT

Supports a between-group comparison across 17 samples.

How we read this: 3 replicated groups read from 17 sample titles; they account for 17 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study
Datasets on a similar topic

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.